Charcot-Marie-Tooth disease axonal type 2L (DOID:0110174)
Alliance: disease page
Synonyms: autosomal dominant axonal Charcot-Marie-Tooth disease type 2L; autosomal dominant Charcot-Marie-Tooth disease type 2L; Charcot-Marie-Tooth neuropathy axonal type 2L; CMT2L
Alt IDs: OMIM:608673, ICD10CM:G60.0, ORDO:99945
Definition: A Charcot-Marie-Tooth disease type 2 that has_material_basis_in mutation in the HSPB8 gene.